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四溴双酚A(TBBPA)通过调节钙离子转运蛋白并导致钙离子稳态失调,诱导TM4支持细胞发生细胞死亡。

Tetrabromobisphenol A (TBBPA), induces cell death in TM4 Sertoli cells by modulating Ca2+ transport proteins and causing dysregulation of Ca2+ homeostasis.

作者信息

Ogunbayo Oluseye A, Lai Pei F, Connolly Thomas J, Michelangeli Francesco

机构信息

School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

出版信息

Toxicol In Vitro. 2008 Jun;22(4):943-52. doi: 10.1016/j.tiv.2008.01.015. Epub 2008 Feb 5.

Abstract

Tetrabromobisphenol A (TBBPA) is a commonly used brominated flame retardant (BFR) utilized to reduce the flammability of a variety of products. Studies have indicated that a number of BFRs are becoming widely distributed within the environment and are bio-accumulating within organisms. There has been much speculation that a variety of phenolic pollutants (including compounds chemically related to TBBPA, such as bisphenol A) may cause endocrine disruption and Ca2+ dysregulation in cells involved in spermatogenesis. In this study we therefore investigate the effects of TBBPA on mouse TM4 Sertoli cells (essential for sperm development). Results show that TBBPA increases Ca2+ within these cells in the 5-60 microM concentration range (EC50, 21 microM). TBBPA also causes cell death (LC50, 18 microM) partly via apoptosis, involving Ca2+-dependent mitochondrial depolarisation. Studies on intracellular Ca2+ transporters shows that TBBPA can inhibit sarcoplasmic/endoplasmic reticulum Ca2+-ATPases (SERCA) at low concentrations (IC50, 0.4 to 1.2 microM) and also activate the Ryanodine receptor Ca2+ channel within the 0.4-4 microM concentration range. Therefore these studies suggest that the cytotoxic effects of TBBPA on cells is partly due to dysregulation of Ca2+ signalling, by directly affecting Ca2+ transport proteins.

摘要

四溴双酚A(TBBPA)是一种常用的溴化阻燃剂(BFR),用于降低各种产品的可燃性。研究表明,许多溴化阻燃剂正在环境中广泛分布,并在生物体内进行生物累积。人们一直在猜测,多种酚类污染物(包括与TBBPA化学相关的化合物,如双酚A)可能会导致参与精子发生的细胞内分泌紊乱和Ca2+调节异常。因此,在本研究中,我们研究了TBBPA对小鼠TM4支持细胞(精子发育所必需的细胞)的影响。结果表明,在5 - 60微摩尔浓度范围内(半数有效浓度,21微摩尔),TBBPA会增加这些细胞内的Ca2+。TBBPA还会部分通过凋亡导致细胞死亡(半数致死浓度,18微摩尔),这涉及Ca2+依赖性线粒体去极化。对细胞内Ca2+转运蛋白的研究表明,TBBPA在低浓度(半数抑制浓度,0.4至1.2微摩尔)时可抑制肌浆网/内质网Ca2+-ATP酶(SERCA),并在0.4 - 4微摩尔浓度范围内激活兰尼碱受体Ca2+通道。因此,这些研究表明,TBBPA对细胞的细胞毒性作用部分是由于直接影响Ca2+转运蛋白而导致Ca2+信号调节异常。

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